FDA 510(k), K123169, ORALID
FDA 510(k), K123169, ORALID
Device Name: ORALID
Manufacturer:
Device Classification Name: Diagnostic Light, Soft Tissue Detector
Regulation Number: 872.6350
Classification Product Code: NXV
Date Received: 10/09/2012
Decision Date: 03/13/2013
Regulation Medical Specialty: Dental
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